Early fetal death associated with compound heterozygosity for Noonan syndrome-causativePTPN11 mutations-Reference-Cited by-同舟云学术

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Early fetal death associated with compound heterozygosity for Noonan syndrome-causativePTPN11 mutations

Published:2007-06-01 Issue:11 Volume:143A Page:1249-1252
ISSN:1552-4825
Container-title:American Journal of Medical Genetics Part A
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Becker Kristin,Hughes Helen,Howard Karol,Armstrong Maggie,Roberts Devender,Lazda Edgar J.,Short John P.,Shaw Adam,Patton Michael A.,Tartaglia Marco

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Reference35 articles.

1. Noonan syndrome: A cryptic condition in early gestation

2. Mouse model of Noonan syndrome reveals cell type– and gene dosage–dependent effects of Ptpn11 mutation

3. The prenatal sonographic features of Noonan's syndrome.

4. Germline Missense Mutations Affecting KRAS Isoform B Are Associated with a Severe Noonan Syndrome Phenotype

5. Juvenile Myelomonocytic Leukemia and Noonan Syndrome

Cited by 8 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Statistical models of the genetic etiology of congenital heart disease;Current Opinion in Genetics & Development;2022-10

2. Extending the prenatal Noonan's phenotype by review of ultrasound and autopsy data;Prenatal Diagnosis;2022-03-22

3. Perinatal features of the RASopathies: Noonan syndrome, Cardiofaciocutaneous syndrome and Costello syndrome;American Journal of Medical Genetics Part A;2014-09-22

4. Juvenile myelomonocytic leukaemia and Noonan syndrome;Journal of Medical Genetics;2014-08-05

5. Atrioventricular canal defect in patients with RASopathies;European Journal of Human Genetics;2012-07-11

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